Apoptosis Apoptosis related

Cat.No.	Name	Information
M9075	Etomoxir sodium salt	Etomoxir((R)-(+)-Etomoxir) sodium salt is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig.
M10566	Valepotriate	Valepotriate has anti-epileptic and anti-cancer activities, it isolated from Valeriana jatamansi Jones.
M7755	Dehydroleucodine	Dehydroleucodine is a sesquiterpene lactone isolated from Artemisia douglasiana Besser; mast cell stabilizers.
M38844	Glyphosate	Glyphosate is an herbicidal derivative of the amino acid glycine. Glyphosate targets and blocks a plant metabolic pathway not found in animals, the shikimate pathway, required for the synthesis of aromatic amino acids in plants.
M4375	Hypericin	Hypericin is an extract of Hypericum perforatum, which has strong antiviral effect and anti-tumor effect.
M53419	Tigapotide	Tigapotide (PCK-3145) is an anti-tumour peptide that reduces the development of skeletal metastases associated with prostate cancer.
M53418	cpm-1285	cpm-1285 induces apoptosis by functionally blocking intracellular Bcl-2 and related death antagonists.
M53417	ABT-510	ABT-510 is an anti-angiogenic TSP peptide (Thrombospondin-1 analogue) that induces apoptosis and inhibits ovarian tumour growth in an orthotopic, syngeneic model of epithelial ovarian cancer.
M53416	HKPao	HKPao (Hunter-killer peptide ao) is a biologically active peptide.
M53415	Kp7-6	Kp7-6, a Fas mimetic peptide, is a Fas/FasL antagonist.
M53414	HXR9	HXR9 is a cell-permeable peptide and a competitive antagonist of HOX/PBX interaction.
M52819	c-JUN peptide	c-JUN peptide is a cell-permeable c-JUN-JNK interaction inhibitor.
M49844	6-Formylpterin	6-Formylpterin is an inhibitor of Xanthine Oxidase. 6-Formylpterin induces intracellular ROS generation and apoptosis in HL-60 cells. 6-Formylpterin suppresses cell proliferation in PanC-1 cells.
M49505	STAT3-IN-9	STAT3-IN-9 is a potent STAT3 inhibitor.
M49504	JAK-2/3-IN-3	JAK-2-/3-IN-3 is a potent JAK2/3 inhibitor with IC50s of 13.00 and 14.86 nM for JAK2 and JAK3, respectively.
M49503	Bozepinib	Bozepinib is a PKR (RNA-dependent protein kinase) activator and potently inhibits the HER-2 signaling pathway as well as JNK and ERK kinases.
M49502	C24:1-Ceramide	C24:1-Ceramide is one of the most abundant naturally occurring ceramide.
M49483	B-355252	B-355252 is a phenoxythiophene sulfonamide small molecule and a potent NGF receptor agonist that enhances NGF-induced neurite growth. It also protects ischemic neurons from neuronal loss by attenuating DNA damage, reducing ROS production and LDH levels, and preventing neuronal apoptosis. In addition, B355252 has anti-apoptotic effects in glutamate-induced excitotoxicity and in a mouse hippocampal cell line (HT22) model of Parkinson's disease (PD).
M44980	Picrasidine Q	Picrasidine Q, an alkaloid component extracted from Angelica keiskei species, has the capacity of anti-cell transformation and anti-cancer.
M44924	Malvidin-3-O-galactoside chloride	Malvidin-3-galactoside chloride, an anthocyanin monomer, induces hepatocellular carcinoma (HCC) cells cycle arrest and apoptosis.
M44795	Biatractylolide	Biatractylolide is a compound isolated from the ethyl acetate extract of Atractylodes macrocephala.
M44780	Apioline	Apiole is an anti-tumor agent that induces apoptosis and inhibits human colon cancer cells by inducing G0/G1 cell cycle arrest.
M44719	3,6-Dihydroxyflavone	3,6-Dihydroxyflavone is an anti-cancer agent.
M44673	(E)-[6]-Dehydroparadol	(E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol (HY-14616), is a potent Nrf2 activator. (E)-[6]-Dehydroparadol can inhibit the growth and induce the apoptosis of human cancer cells.
M43377	PI3Kδ-IN-16	PI3Kδ-IN-16 is a potent and selective inhibitor of PI3Kδ.

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